Linked Data
dbSNP Id:
rs2057543927
gnomAD v4:
3-12532719-T-TA
MyVariant Identifiers:
chr3:g.12574218_12574219insA (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.12532721dup , CM000665.2:g.12532721dup | GRCh38 |
| NC_000003.11:g.12574220dup , CM000665.1:g.12574220dup | GRCh37 |
| NC_000003.10:g.12549220dup | NCBI36 |
| NG_011521.1:g.53290dup | |
| NG_011521.2:g.53290dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000284995.11:c.1398dup (TSEN2) MANE Select | ENSP00000284995.6:n.1398dup | |
| ENST00000412698.3:c.1260+1062dup (TSEN2) | ENSP00000408528.3:n.1260+1062dup | |
| ENST00000415684.6:c.1320dup (TSEN2) | ENSP00000416510.1:n.1320dup | |
| ENST00000444864.6:c.1260+1062dup (TSEN2) | ENSP00000407974.2:n.1260+1062dup | |
| ENST00000446004.6:c.1338+1062dup (TSEN2) | ENSP00000406238.2:n.1338+1062dup | |
| ENST00000455118.6:c.*239dup (TSEN2) | ENSP00000408744.2:n.*239dup | |
| ENST00000475595.2:n.4081dup (TSEN2) | ||
| ENST00000679367.1:c.*1017dup (TSEN2) | ENSP00000506510.1:n.*1017dup | |
| ENST00000679420.1:n.1571dup (TSEN2) | ||
| ENST00000679424.1:c.*1241dup (TSEN2) | ENSP00000505917.1:n.*1241dup | |
| ENST00000679425.1:c.1398dup (TSEN2) | ENSP00000505890.1:n.1398dup | |
| ENST00000679492.1:c.1338+1062dup (TSEN2) | ENSP00000505331.1:n.1338+1062dup | |
| ENST00000679555.1:c.*1121dup (TSEN2) | ENSP00000505538.1:n.*1121dup | |
| ENST00000679670.1:c.1320dup (TSEN2) | ENSP00000506080.1:n.1320dup | |
| ENST00000679690.1:c.*397dup (TSEN2) | ENSP00000506383.1:n.*397dup | |
| ENST00000679693.1:c.*175+1062dup (TSEN2) | ENSP00000505108.1:n.*175+1062dup | |
| ENST00000679699.1:c.1398dup (TSEN2) | ENSP00000505274.1:n.1398dup | |
| ENST00000679756.1:c.1347dup (TSEN2) | ENSP00000506391.1:n.1347dup | |
| ENST00000679785.1:c.*239dup (TSEN2) | ENSP00000506473.1:n.*239dup | |
| ENST00000679835.1:c.*587dup (TSEN2) | ENSP00000505616.1:n.*587dup | |
| ENST00000679876.1:c.1209+1062dup (TSEN2) | ENSP00000504930.1:n.1209+1062dup | |
| ENST00000679995.1:c.*239dup (TSEN2) | ENSP00000505221.1:n.*239dup | |
| ENST00000680126.1:c.*1237dup (TSEN2) | ENSP00000505345.1:n.*1237dup | |
| ENST00000680264.1:c.*527+1062dup (TSEN2) | ENSP00000505273.1:n.*527+1062dup | |
| ENST00000680275.1:c.1455dup (TSEN2) | ENSP00000505417.1:n.1455dup | |
| ENST00000680354.1:c.1377dup (TSEN2) | ENSP00000505106.1:n.1377dup | |
| ENST00000680376.1:c.*587dup (TSEN2) | ENSP00000506369.1:n.*587dup | |
| ENST00000680421.1:c.1269dup (TSEN2) | ENSP00000505530.1:n.1269dup | |
| ENST00000680449.1:c.*540dup (TSEN2) | ENSP00000505709.1:n.*540dup | |
| ENST00000680458.1:c.*213dup (TSEN2) | ENSP00000505979.1:n.*213dup | |
| ENST00000680555.1:c.*239dup (TSEN2) | ENSP00000505160.1:n.*239dup | |
| ENST00000680598.1:c.1347dup (TSEN2) | ENSP00000506297.1:n.1347dup | |
| ENST00000680765.1:c.*239dup (TSEN2) | ENSP00000505351.1:n.*239dup | |
| ENST00000680817.1:c.1269dup (TSEN2) | ENSP00000506221.1:n.1269dup | |
| ENST00000680857.1:c.1338+1062dup (TSEN2) | ENSP00000506578.1:n.1338+1062dup | |
| ENST00000680873.1:c.*550dup (TSEN2) | ENSP00000505233.1:n.*550dup | |
| ENST00000680923.1:c.*587dup (TSEN2) | ENSP00000505344.1:n.*587dup | |
| ENST00000680943.1:c.1347dup (TSEN2) | ENSP00000505442.1:n.1347dup | |
| ENST00000680986.1:c.1398dup (TSEN2) | ENSP00000505799.1:n.1398dup | |
| ENST00000681042.1:c.1100-6440dup (TSEN2) | ENSP00000505622.1:n.1100-6440dup | |
| ENST00000681073.1:c.*239dup (TSEN2) | ENSP00000506576.1:n.*239dup | |
| ENST00000681140.1:c.1398dup (TSEN2) | ENSP00000505099.1:n.1398dup | |
| ENST00000681227.1:c.*270dup (TSEN2) | ENSP00000505240.1:n.*270dup | |
| ENST00000681268.1:c.*1542dup (TSEN2) | ENSP00000505385.1:n.*1542dup | |
| ENST00000681343.1:c.*1017dup (TSEN2) | ENSP00000506265.1:n.*1017dup | |
| ENST00000681433.1:c.*239dup (TSEN2) | ENSP00000505729.1:n.*239dup | |
| ENST00000681471.1:c.1320dup (TSEN2) | ENSP00000505105.1:n.1320dup | |
| ENST00000681482.1:c.1398dup (TSEN2) | ENSP00000505436.1:n.1398dup | |
| ENST00000681676.1:c.1320dup (TSEN2) | ENSP00000506163.1:n.1320dup | |
| ENST00000681713.1:c.*1017dup (TSEN2) | ENSP00000506046.1:n.*1017dup | |
| ENST00000284995.10:c.1398dup (TSEN2) | ENSP00000284995.6:n.1398dup | |
| ENST00000402228.7:c.1398dup (TSEN2) | ENSP00000385976.3:n.1398dup | |
| ENST00000412698.2:c.93+1062dup (TSEN2) | ENSP00000408528.2:n.93+1062dup | |
| ENST00000415684.5:c.1320dup (TSEN2) | ENSP00000416510.1:n.1320dup | |
| ENST00000454502.6:c.1221dup (TSEN2) | ENSP00000392029.2:n.1221dup | |
| ENST00000455118.5:c.245dup (TSEN2) | ||
| ENST00000473755.5:n.3403dup (TSEN2) | ||
| ENST00000475595.1:n.244dup (TSEN2) | ||
| ENST00000567514.1:n.715+6787dup (MKRN2OS) | ||
| NM_001145392.1:c.1398dup (TSEN2) | NP_001138864.1:n.1398dup | |
| NM_001145393.1:c.1320dup (TSEN2) | NP_001138865.1:n.1320dup | |
| NM_001145394.1:c.1221dup (TSEN2) | NP_001138866.1:n.1221dup | |
| NM_025265.3:c.1398dup (TSEN2) | NP_079541.1:n.1398dup | |
| XM_005265495.1:c.1398dup (TSEN2) | XP_005265552.1:n.1398dup | |
| XM_005265497.1:c.1320dup (TSEN2) | XP_005265554.1:n.1320dup | |
| XM_005265498.1:c.1269dup (TSEN2) | XP_005265555.1:n.1269dup | |
| XM_011534138.1:c.1131dup (TSEN2) | XP_011532440.1:n.1131dup | |
| XM_011534139.1:c.1125dup (TSEN2) | XP_011532441.1:n.1125dup | |
| XR_245158.1:n.1501dup (TSEN2) | ||
| XR_245159.3:n.1501dup (TSEN2) | ||
| XR_427295.2:n.3403dup (TSEN2) | ||
| XR_427296.1:n.1311dup (TSEN2) | ||
| NM_001145393.2:c.1320dup (TSEN2) | NP_001138865.1:n.1320dup | |
| NM_001321277.1:c.1398dup (TSEN2) | NP_001308206.1:n.1398dup | |
| NM_001321278.1:c.1338+1062dup (TSEN2) | NP_001308207.1:n.1338+1062dup | |
| NM_001321279.1:c.1320dup (TSEN2) | NP_001308208.1:n.1320dup | |
| NR_135607.1:n.1501dup (TSEN2) | ||
| XM_011534139.3:c.1125dup (TSEN2) | XP_011532441.1:n.1125dup | |
| XM_017007292.1:c.1455dup (TSEN2) | XP_016862781.1:n.1455dup | |
| XM_017007293.1:c.1455dup (TSEN2) | XP_016862782.1:n.1455dup | |
| XM_017007294.1:c.1455dup (TSEN2) | XP_016862783.1:n.1455dup | |
| XM_017007295.2:c.1455dup (TSEN2) | XP_016862784.1:n.1455dup | |
| XM_017007296.2:c.1398dup (TSEN2) | XP_016862785.1:n.1398dup | |
| XM_017007297.1:c.1377dup (TSEN2) | XP_016862786.1:n.1377dup | |
| XM_024453785.1:c.1320dup (TSEN2) | XP_024309553.1:n.1320dup | |
| XR_001740287.1:n.1842dup (TSEN2) | ||
| XR_001740288.2:n.1842dup (TSEN2) | ||
| XR_001740289.2:n.1785dup (TSEN2) | ||
| XR_001740290.2:n.1399dup (TSEN2) | ||
| XR_001740291.1:n.1707dup (TSEN2) | ||
| XR_001740292.1:n.1805dup (TSEN2) | ||
| XR_001740293.1:n.1805dup (TSEN2) | ||
| XR_001740294.2:n.1440dup (TSEN2) | ||
| XR_001740295.2:n.1362dup (TSEN2) | ||
| XR_001740296.1:n.1652dup (TSEN2) | ||
| XR_001740297.1:n.1970dup (TSEN2) | ||
| XR_001740298.2:n.1287dup (TSEN2) | ||
| XR_001740300.2:n.1605dup (TSEN2) | ||
| XR_001740301.2:n.1605dup (TSEN2) | ||
| XR_001740302.2:n.1568dup (TSEN2) | ||
| XR_001740303.2:n.1415dup (TSEN2) | ||
| XR_001740304.1:n.1723dup (TSEN2) | ||
| XR_002959592.1:n.1576dup (TSEN2) | ||
| XR_002959593.1:n.1533dup (TSEN2) | ||
| XR_002959594.1:n.1573dup (TSEN2) | ||
| XR_002959595.1:n.1913dup (TSEN2) | ||
| XR_427296.2:n.1287dup (TSEN2) | ||
| NM_001321278.2:c.1338+1062dup (TSEN2) | NP_001308207.1:n.1338+1062dup | |
| NM_025265.4:c.1398dup (TSEN2) MANE Select | NP_079541.1:n.1398dup | |
| NR_135607.2:n.1453dup (TSEN2) | ||
| NM_001145392.2:c.1398dup (TSEN2) | NP_001138864.1:n.1398dup | |
| NM_001145393.3:c.1320dup (TSEN2) | NP_001138865.1:n.1320dup | |
| NM_001145394.2:c.1221dup (TSEN2) | NP_001138866.1:n.1221dup | |
| NM_001321277.2:c.1398dup (TSEN2) | NP_001308206.1:n.1398dup | |
| NM_001321279.2:c.1320dup (TSEN2) | NP_001308208.1:n.1320dup |